ENT-single-use suction tubes, angled

FDA UDI

Class II (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name: ENT-single-use suction tubes, angled FDA UDI
Generic Name: Suction/irrigation tubing, single-use FDA UDI
Device Name: suction control on top 120x3.0 mm, sterile, 50 pieces/box FDA UDI
Model / Reference: 3012030 FDA UDI
Description: suction control on top 120x3.0 mm, sterile, 50 pieces/box FDA UDI

Identifiers

Catalog Number: 3012030 FDA UDI
Primary DI / UDI-DI: 04250381814994 FDA UDI
FDA Product Code: BYY FDA UDI
GMDN Term: Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction/irrigation tubing, single-use

ENT-single-use suction tubes, angled by Spiggle & Theis Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Suction/irrigation tubing, single-use.

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Suction Tube Ch 24, 350 cm — Dispo Medical B.V. · Class I
Bioseal Inc. — BIOSEAL · Class I
BHL-SuctionCare — BHL-Medical, Indústria de Produtos Hospitalares, lda · Class I
CARDINAL HEALTH — Cardinal Health 200, LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Spiggle & Theis Medizintechnik GmbH

Sources (1)

FDA UDI 6841dca7-9b3f-4d84-812f-7ffca3b256bb 35 fields · synced Jun 8, 2026